Ethylene Glycol → HCID 86744497, compound
Reaction equation
[CH2:1]([OH:4])[CH2:2][OH:3].S(Cl)([Cl:7])=O.[C:9](O)(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[N:12][CH:11]=1>O1CCCC1>[ClH:7].[OH:3][CH2:2][CH2:1][O:4][C:9]([C:10]1[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=1)=[O:16]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To 120 mL cold (-10° C.) ethylene glycol, 16 mL of thionyl chloride were added dropwise. Upon completion of the addition, 24.6 g (0.2 mol) of nicotinic acid were added portionwise and the reaction mixture was heated overnight at 60° C. Then, 700 mL of hot tetrahydrofuran were added and the mixture was cooled. The solid which formed was removed by filtration and washed with ether to give 28.5 g of the title compound as white crystals.
Workup
- additionwere added portionwise
- temperaturethe mixture was cooled
- customThe solid which formed
- customwas removed by filtration
- washwashed with ether
Sources & evidence
- ORD record
- ord-d6e365e6326d48dd85d0d17fdf0a8259
- Source dataset
- uspto-grants-1991_03
- Patent number
- US05002935
Reaction notes
Loading…